PMA supplement
P060038 S002: MITROFLOW AORTIC PERICARDIAL HEART VALVE MODEL LX
FDA PMA supplement · Real-Time Process · Corcym Canada Corp
Key facts
| Original PMA | P060038 |
|---|---|
| Supplement number | S002 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | MITROFLOW AORTIC PERICARDIAL HEART VALVE MODEL LX |
| Generic name | Heart-valve, non-allograft tissue |
| Applicant | Corcym Canada Corp |
| Product code | LWR |
| Received date | Dec 29, 2008 |
| Decision date | Feb 27, 2009 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: